Basic information
- Standard SMILES
CC(=N[Si](C)(C)C)O[Si](C)(C)C- InChIKey
SIOVKLKJSOKLIF-UHFFFAOYSA-N- Molecular formula
- C8H21NOSi2
- Average molar mass
- 203.43 g/mol
- Monoisotopic mass
- 203.11616735
Names & identifiers
- Preferred name
- trimethylsilyl N-trimethylsilylethanimidate
- IUPAC
- trimethylsilyl N-trimethylsilylethanimidate
- English name
- N,O-Bis(trimethylsilyl)acetamide
- Molecular formula
- C8H21NOSi2
- Molecular weight
- 203.43
Names & synonyms
Show more names
Database identifiers
- CAS
10416-59-8- PubChem CID
- 25248
- DTXSID
DTXSID5051525
Properties
Computed structural properties
- Topological polar surface area
- 21.6 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 2
- Rotatable bonds
- 3
- Heavy atoms
- 12
- Formal charge
- 0
- Complexity
- 176
Experimental & physicochemical properties
Physicochemical properties
- Melting point
- 24 °C · 24 °C
- Boiling point
- 71 · 71-73 °C35 mm Hg(lit.)
- Density
- 0.832 g/mL · 0.832 g/mL at 20 °C(lit.)
- vapor pressure
- 10 hPa · 10 hPa (50 °C)
- refractive index
- 20 · n20/D 1.417(lit.)
- Flash point
- 53 °F · 53 °F
- storage temp.
- 30 °C · Store below +30°C.
- solubility
- Miscible with many nonpolar and polar aprotic solvents.
- form
- Crystalline Powder, Crystals and/or Chunks
- pka
- 5.82 · 5.82±0.50(Predicted)
- Specific Gravity
- 0.832 · 0.832
- color
- Light yellow or beige to brown
- Hydrolytic Sensitivity
- 7 · 7: reacts slowly with moisture/water
- Sensitive
- Moisture Sensitive
- BRN
- 1306669 · 1306669
- InChI
- 1S/C8H21NOSi2/c1-8(9-11(2,3)4)10-12(5,6)7/h1-7H3/b9-8+
- InChIKey
- SIOVKLKJSOKLIF-CMDGGOBGSA-N
- SMILES
- C\C(O[Si](C)(C)C)=N/[Si](C)(C)C
- CAS DataBase Reference
- 10416 · 10416-59-8(CAS DataBase Reference)
- EWG's Food Scores
- 1 · 1
- FDA UNII
- 14 N49I64O · R14N49I64O
- NIST Chemistry Reference
- Ethanimidic acid, N-(trimethylsilyl)-, trimethylsilyl ester(10416-59-8)
- EPA Substance Registry System
- Ethanimidic acid, N-(trimethylsilyl)-, trimethylsilyl ester (10416-59-8)
- UNSPSC Code
- 41116105 · 41116105
- NACRES
- 22 · NA.22
- Symbol(GHS)
- 2 · GHS02,GHS05,GHS07
- Signal word
- Danger
- Hazard statements
- 226 · H226-H302-H314
- Precautionary statements
- 210 · P210-P233-P280-P301+P312-P303+P361+P353-P305+P351+P338
- PPE
- 3 · Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
- Hazard Codes
- C,Xn,F
- Risk Statements
- 10 · 10-14-22-34-40-20/21/22-11
- Safety Statements
- 26 · 26-36/37/39-45-7/8-43A-36-30-23-16-7/9
- RIDADR
- 2920 · UN 2920 8/PG 2
- WGK Germany
- 3 · 3
- RTECS
- 3000000 · AK3000000
- F
- 10 · 10-21
- TSCA
- TSCA listed
- HazardClass
- 8 · 8
- PackingGroup
- II
- HS Code
- 29310095 · 29310095
- Storage Class
- 3 · 3 - Flammable liquids
- Hazard Classifications
- 4 OralFlam · Acute Tox. 4 OralFlam. Liq. 3Skin Corr. 1B
- Toxicity
- 50 orally · LD50 orally in Rabbit: 1580 mg/kg
- REACH Registrations
- Active
- Limited Quantities
- 1 L · 1.0 L (0.3 gallon) (liquid)
- Excepted Quantities
- Max Inner Pack (30g or 30ml) and Max Outer Pack (500g or 500ml)
Safety & regulation
Safety data
- F
- 10-21
- PPE
- Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
- wgk
- 3
- tsca
- TSCA listed
- rtecs
- AK3000000
- ridadr
- UN 2920 8/PG 2
- hs_code
- 29310095
- Toxicity
- LD50 orally in Rabbit: 1580 mg/kg
- risk_code
- 10-14-22-34-40-20/21/22-11
- Signal word
- Danger
- Symbol(GHS)
- GHS02,GHS05,GHS07
- hazard_code
- C,Xn,F
- safety_code
- 26-36/37/39-45-7/8-43A-36-30-23-16-7/9
- hazard_class
- 8
- Storage Class
- 3 - Flammable liquids
- packing_group
- II
- Hazard statements
- H226-H302-H314
- Limited Quantities
- 1.0 L (0.3 gallon) (liquid)
- Excepted Quantities
- Max Inner Pack (30g or 30ml) and Max Outer Pack (500g or 500ml)
- REACH Registrations
- Active
- Hazard Classifications
- Acute Tox. 4 OralFlam. Liq. 3Skin Corr. 1B
- Precautionary statements
- P210-P233-P280-P301+P312-P303+P361+P353-P305+P351+P338
Chemistry & industry
Applications
DescriptionClear to yellowish clear liquid liquid which is soluble in many nonpolar and polar aprotic solvents. The trimethylsilyl group is a frequently utilized monofunctional blocking group for protic organic and inorganic materials. As it eliminated during the silylation is neutral acetamide, N,O-Bis(trimethylsilyl)acetamide can be preferably used for substrates which are acid- or base-sensitive. N,O-bis(trimethylsilyl)-acetamide is an effective silylating agent. It is used in the pharmaceutical and in the chemical industry. Typically the silylating reaction with BSA results in neutral by-products only.
UsesUsed for blocking and protection of hydroxyl groups in natural products, e.g. amino acids, carbohydrates; Used for blocking and protection of functional groups in organic intermediates; Used for formation of derivatives of H-acid compounds for analysis; The silylated derivatives are volatile and can therefore be determined by gas chromatography. Deblocking is preferably carried out by means of hydrolysis, giving high yields. In some cases, thermal elimination of the trimethylsilyl group is possible.
UsesPowerful silylation reagent for a wide range of functional groups under mild conditions
UsesN,O-bis(trimethylsilyl)-acetamide (BSA) is frequently used with TMCS as a catalyst to modify a variety of functional groups including carboxyl groups. In one novel application, BSA was used to measure carboxypeptidase activity by forming derivatives which could be determined by gas chromatography.BSA has been used to prepare derivatives of steroids and glucocorticoids.
UsesN,O-Bis(trimethylsilyl)acetamide is a powerful silylating agent; reacts with a wide range of functional groups.BSA was used to trimethylsilylate the hydroxyl group of 12 selectively to form in almost quantitative yield (eq 32).The presence of catalytic amounts (~0.02 equiv) of tetrabutylammonium fluoride (TBAF) significantly promoted the silylation of alcohols under mild conditions with high chemoselectivity, i.e., TBAF plays a role as a smooth silyl transfer catalyst from nitrogen to the hydroxyl group.
General DescriptionN,O-Bis(trimethylsilyl)acetamide is an excellent silylation reagent. For some sterically hindered primary or secondary nitro compounds, N,O-bis(trimethylsilyl)acetamide and BSTFA achieve better results than normal silylation conditions.
Preparation methods
PreparationN,O-Bis(trimethylsilyl)acetamide is made by the reaction of acetamide with a large excess of chlorotrimethylsilane in the presence of triethylamine.
Upstream & downstream products
Upstream raw materials
Downstream products
Suppliers50 total
Related reactions
Linked notes
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